Canonical Allele Identifier: CA2200882983
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176943_176946delinsTCCC , CM000678.2:g.176943_176946delinsTCCC GRCh38
NC_000016.9:g.226942_226945delinsTCCC , CM000678.1:g.226942_226945delinsTCCC GRCh37
NC_000016.8:g.166942_166945delinsTCCC NCBI36
NG_000006.1:g.37806_37809delinsTCCC
NG_059186.1:g.5293_5296delinsTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.110_113delinsTCCC MANE Select ENSP00000322421.5:p.Phe37=
ENST00000397797.1:c.14_17delinsTCCC ENSP00000380899.1:p.Phe5=
ENST00000472694.1:n.246_249delinsTCCC
ENST00000487791.1:n.79_82delinsTCCC
NM_000558.4:c.110_113delinsTCCC NP_000549.1:p.Phe37=
NM_000558.5:c.110_113delinsTCCC MANE Select NP_000549.1:p.Phe37=